A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18273282



Internal ID20840322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:2835513..2836613hg38UCSC Ensembl
chr6:2835747..2836847hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg381101
hg191101
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6567763
Supporting Variants
Samples
Known GenesSERPINB1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18273282
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.0001


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